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Vista de la lista Vista de las tarjetas
  • Dispositivo 333
  • Fabricante 333
  • Evento 349
  • Implante 0
Medtronic Advanced Energy LLC
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
N/A
  • Source
    NOM
INTCO INDUSTRIES Co. Ltd, China
  • Source
    NOM
Albomed GmbH
  • Source
    NOM
ANGIPLAST – INDIA.
  • Source
    NOM
Arista Latindo, Indonesia
  • Representante del fabricante
    Distributor: "DUCASCO" DURMOUSOGLOU AEVE
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
Depuy Mitek
  • Empresa matriz del fabricante (2017)
    Johnson & Johnson
  • Source
    NOM
ETHICON ENDO SURGERY (EUROPE) GmbH
  • Empresa matriz del fabricante (2017)
    Johnson & Johnson
  • Source
    NOM
MEDTRONIC
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    NOM
Abbott Vascular
  • Empresa matriz del fabricante (2017)
    Abbott Laboratories
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    NOM
Alere Medical Co., Ltd - Japan
  • Empresa matriz del fabricante (2017)
    Abbott Laboratories
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    NOM
Diagnostik Nord GmbH
  • Empresa matriz del fabricante (2017)
    Abbott Laboratories
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    NOM
AFP Medical, UK
  • Empresa matriz del fabricante (2017)
    Afp Medical Limited
  • Source
    NOM
DAKO DENMARK A/S
  • Empresa matriz del fabricante (2017)
    Agilent Technologies, Inc.
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
ALPHA-BIO TEC. LTD., Israel
  • Empresa matriz del fabricante (2017)
    Alpha - Bio Tec. Ltd
  • Source
    NOM
ANGIODYNAMICS
  • Empresa matriz del fabricante (2017)
    AngioDynamics Inc
  • Source
    NOM
AngioDynamics, Inc.
  • Empresa matriz del fabricante (2017)
    AngioDynamics Inc
  • Source
    NOM
Anhui Kangda Medical Products Co
  • Empresa matriz del fabricante (2017)
    Anhui Kangda Medical Products Co. Ltd.
  • Source
    NOM
Applied Medical Technology Inc.
  • Empresa matriz del fabricante (2017)
    Applied Medical Technology Inc.
  • Source
    NOM
ARKRAY Factory, Inc.
  • Empresa matriz del fabricante (2017)
    Arkray Inc.
  • Source
    NOM
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.